SRGAP3
SLIT-ROBO Rho GTPase activating protein 3
Summary
Predicted to enable GTPase activator activity. Predicted to be involved in negative regulation of cell migration and regulation of postsynapse assembly. Is active in postsynapse. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants103 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs770690937 | 3:9,027,231 | C/A | — | uncertain significance |
| rs3732978 | 3:9,027,262 | C/T | — | benign |
| rs144096171 | 3:9,027,281 | C/T | — | likely benign |
| rs1482076914 | 3:9,027,307 | G/A | — | uncertain significance |
| rs373709294 | 3:9,027,325 | C/A | — | uncertain significance |
| rs766810764 | 3:9,027,337 | G/T | — | uncertain significance |
| rs760093750 | 3:9,027,340 | G/A | — | uncertain significance |
| rs748187826 | 3:9,027,371 | G/A | — | likely benign |
| rs1488419249 | 3:9,027,426 | C/T | — | uncertain significance |
| rs1941661638 | 3:9,027,433 | C/A | — | uncertain significance |
| rs61747989 | 3:9,027,467 | G/A | — | benign |
| rs138360684 | 3:9,032,211 | G/A | — | likely benign |
| rs146287162 | 3:9,032,265 | C/T | — | benign |
| rs144015894 | 3:9,032,321 | C/T | — | uncertain significance |
| rs1177312003 | 3:9,032,347 | C/T | — | uncertain significance |
| rs768132072 | 3:9,032,350 | T/C | — | uncertain significance |
| rs764823026 | 3:9,032,387 | T/A | — | uncertain significance |
| rs200165462 | 3:9,032,402 | T/C | — | benign |
| rs754547731 | 3:9,032,419 | C/T | — | uncertain significance |
| rs780791582 | 3:9,032,420 | G/A | — | uncertain significance |
| rs769562773 | 3:9,032,428 | G/A | — | uncertain significance |
| rs984806535 | 3:9,032,448 | G/T | — | likely benign |
| rs780736446 | 3:9,032,482 | C/T | — | uncertain significance |
| rs373938230 | 3:9,032,503 | C/G | — | uncertain significance |
| rs201629131 | 3:9,034,594 | C/T | — | uncertain significance |
| rs150617309 | 3:9,034,605 | C/T | — | likely benign |
| rs146843771 | 3:9,034,613 | A/G | — | benign |
| rs953053584 | 3:9,034,723 | C/G | — | uncertain significance |
| rs774821102 | 3:9,034,739 | C/T | — | uncertain significance |
| rs116480276 | 3:9,036,059 | G/A | — | benign |
| rs2469939118 | 3:9,036,061 | G/C | — | uncertain significance |
| rs772781725 | 3:9,036,082 | G/A | — | uncertain significance |
| rs770659662 | 3:9,036,101 | C/T | — | likely benign |
| rs1033693138 | 3:9,036,154 | G/A | — | likely pathogenic |
| rs748768469 | 3:9,036,159 | G/C | — | uncertain significance |
| rs771899704 | 3:9,036,193 | C/G | — | uncertain significance |
| rs371916241 | 3:9,036,213 | A/G | — | likely benign |
| rs761802559 | 3:9,052,040 | C/T | — | uncertain significance |
| rs763116513 | 3:9,052,055 | C/T | — | uncertain significance |
| rs76476731 | 3:9,052,056 | G/A | — | benign |
| rs377512438 | 3:9,055,014 | T/C | — | uncertain significance |
| rs1488291388 | 3:9,055,064 | G/A | — | uncertain significance |
| rs201964498 | 3:9,055,147 | C/A | — | uncertain significance |
| rs375152533 | 3:9,055,412 | G/C | — | likely benign |
| rs918548062 | 3:9,055,434 | C/T | — | uncertain significance |
| rs145531861 | 3:9,055,435 | G/A | — | likely benign |
| rs2271207 | 3:9,055,458 | T/C | — | benign |
| rs748427822 | 3:9,055,480 | G/A | — | likely benign |
| rs141284390 | 3:9,057,396 | G/A | — | likely benign |
| rs2470113517 | 3:9,066,951 | C/G | — | uncertain significance |
| rs750611694 | 3:9,068,621 | T/C | — | uncertain significance |
| rs79362157 | 3:9,068,656 | A/C | — | benign |
| rs1333216544 | 3:9,074,403 | C/A | — | uncertain significance |
| rs376576758 | 3:9,074,420 | G/A | — | uncertain significance |
| rs2470197212 | 3:9,079,766 | C/T | — | uncertain significance |
| rs2292251 | 3:9,089,065 | G/C | — | benign |
| rs910578733 | 3:9,089,086 | G/A | — | uncertain significance |
| rs1305207359 | 3:9,089,130 | G/T | — | uncertain significance |
| rs79582857 | 3:9,092,886 | A/T | intron variant | — |
| rs370075635 | 3:9,094,712 | G/A | — | uncertain significance |
| rs1945659937 | 3:9,094,748 | C/T | — | uncertain significance |
| rs762093906 | 3:9,094,771 | G/C | — | uncertain significance |
| rs34036997 | 3:9,094,822 | G/A | — | likely benign |
| rs185541928 | 3:9,094,870 | C/T | — | likely benign |
| rs760145287 | 3:9,097,930 | A/G | — | uncertain significance |
| rs61747290 | 3:9,099,983 | G/C | — | benign |
| rs112559195 | 3:9,099,987 | T/A | — | likely benign |
| rs61747289 | 3:9,099,989 | G/A | — | benign |
| rs2470326682 | 3:9,100,000 | C/T | — | uncertain significance |
| rs779206383 | 3:9,100,023 | C/T | — | uncertain significance |
| rs61745234 | 3:9,100,088 | G/A | — | benign |
| rs759170968 | 3:9,100,100 | T/A | — | likely benign |
| rs754715058 | 3:9,101,918 | G/A | — | likely benign |
| rs769568751 | 3:9,101,937 | T/C | — | uncertain significance |
| rs2470343619 | 3:9,101,953 | T/C | — | uncertain significance |
| rs143061036 | 3:9,101,963 | G/A | — | likely benign |
| rs1560040068 | 3:9,101,998 | G/A | — | uncertain significance |
| rs1256071261 | 3:9,102,006 | G/A | — | uncertain significance |
| rs35952589 | 3:9,102,016 | G/A | — | benign |
| rs530930175 | 3:9,106,091 | T/G | — | uncertain significance |
| rs149157821 | 3:9,106,120 | C/T | — | uncertain significance |
| rs141577564 | 3:9,106,129 | C/T | — | uncertain significance |
| rs201116450 | 3:9,106,137 | G/A | — | likely benign |
| rs201104166 | 3:9,106,146 | C/T | — | likely benign |
| rs146407315 | 3:9,106,221 | C/T | — | benign |
| rs374698201 | 3:9,121,750 | T/G | — | uncertain significance |
| rs754930892 | 3:9,121,758 | C/T | — | uncertain significance |
| rs1575041345 | 3:9,121,778 | T/C | — | likely benign |
| rs546500934 | 3:9,122,355 | G/A | — | — |
| rs544274585 | 3:9,142,025 | C/A | — | — |
| rs368369285 | 3:9,146,401 | G/T | — | uncertain significance |
| rs372381347 | 3:9,146,411 | C/T | — | uncertain significance |
| rs757456083 | 3:9,146,472 | C/T | — | likely benign |
| rs768436049 | 3:9,166,433 | C/T | — | uncertain significance |
| rs201463303 | 3:9,166,445 | G/A | — | uncertain significance |
| rs138801402 | 3:9,166,498 | A/C | — | likely benign |
| rs1575110501 | 3:9,166,519 | C/T | — | likely benign |
| rs778613060 | 3:9,166,573 | G/T | — | uncertain significance |
| rs758150937 | 3:9,166,584 | C/T | — | uncertain significance |
| rs377253106 | 3:9,290,560 | G/T | — | likely benign |
Showing 100 of 103 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.